Publication: Freeman-Sheldon Syndrome Associated with Hemophilia-A in a Newborn
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Date
2016-12-01T00:00:00Z
Authors
BAYRAKTAR, Bilge
Bayraktar, Suleyman
ARSLAN, HÜSEYİN
ÇAKIR, FATMA BETÜL
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Abstract
The Freeman-Sheldon syndrome (FSS) (whistling face) is a congenital autosomal dominant disease (rarely described in its autosomal recessive form) characterized by small -whistling- mouth, a flat masklike face, joint contractures (commonly involving the fingers and hands) and underdevelopment of the nasal cartilage. Other clinical features include full forehead, deep set eyes, epicanthal folds, high palate, H-shaped cutaneous dimpling on the chin, ulnar deviation of the hands, seizures, and dislocation of the hip. A 10-day-old male newborn was admitted to our neonatal intensive care unit with jaundice and hyperthermia. He had fever of 42.5 degrees C, small whistling mouth, a flat mask-like face, joint contractures of the fingers, and ulnar deviation of the hands. The parents were consanguineous and one of the boys died when he was 1 years old due to intracranial hemorrhage. To our knowledge, there have been more than 60 cases diagnosed with FSS. This is the first reported case of Freeman-Sheldon syndrome associated with hemophilia A and the second case of FSS associated with fever without anesthesia.
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BAYRAKTAR B., Bayraktar S., ARSLAN H., ÇAKIR F. B. , -Freeman-Sheldon Syndrome Associated with Hemophilia-A in a Newborn-, HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI, cilt.54, ss.243-245, 2016